Standout Papers
- Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23 (2000)
- Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2 (2004)
- An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita (1994)
- Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine (2005)
- Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism (1994)
Immediate Impact
15 by Nobel laureates 15 from Science/Nature 66 standout
Citing Papers
Gene Editing for CEP290 -Associated Retinal Degeneration
2024 Standout
The extracellular matrix and the immune system: A mutually dependent relationship
2023 StandoutScience
Works of Tim M. Strom being referenced
Time‐ and compartment‐resolved proteome profiling of the extracellular niche in lung injury and repair
2015
Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis
2006
Author Peers
| Author | Last Decade | Papers | Cites | |||
|---|---|---|---|---|---|---|
| Tim M. Strom | 7869 | 5846 | 3437 | 215 | 16.2k | |
| Thomas Meitinger | 11034 | 5431 | 1689 | 314 | 18.7k | |
| Allen M. Spiegel | 9906 | 2679 | 3137 | 290 | 18.8k | |
| Geoffrey N. Hendy | 5091 | 2126 | 3385 | 238 | 10.5k | |
| Thomas E. Willnow | 6713 | 1474 | 1342 | 178 | 14.5k | |
| Peter Mündel | 8238 | 3201 | 12610 | 157 | 19.7k | |
| Keiichi Ozono | 4059 | 2278 | 1207 | 424 | 10.3k | |
| Yo‐ichi Nabeshima | 4789 | 3161 | 3190 | 118 | 10.0k | |
| William J. Pavan | 5944 | 1765 | 1750 | 222 | 13.3k | |
| Leonard J. Deftos | 3760 | 1010 | 1303 | 278 | 10.7k | |
| John M. Shelton | 15441 | 2767 | 544 | 151 | 22.4k |
All Works
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